126 related articles for article (PubMed ID: 38411002)
21. Iris Heterochromia and Choroidal Hypopigmentation in Waardenburg Syndrome.
Park JG; Randhawa S; Capone A
Ophthalmology; 2023 Jan; 130(1):55. PubMed ID: 35773070
[No Abstract] [Full Text] [Related]
22. The clinical and genetic research of Waardenburg syndrome type I and II in Chinese families.
Liu Q; Cheng J; Lu Y; Zhou J; Wang L; Yang C; Yang G; Yang H; Cao J; Zhang Z; Sun Y
Int J Pediatr Otorhinolaryngol; 2020 Mar; 130():109806. PubMed ID: 31812001
[TBL] [Abstract][Full Text] [Related]
23. A Novel Variant in Paired Box 3 Gene-related with Waardenburg Syndrome Type-1 in an Afghan Family.
Dogan M; Eroz R
J Coll Physicians Surg Pak; 2022 Aug; 32(8):S110-S112. PubMed ID: 36210664
[TBL] [Abstract][Full Text] [Related]
24. [Ophthalmologic manifestations of Waardenburg syndrome].
Astakhov YS; Tultseva SN; Lisochkina AB; Takhtaev YV; Astakhov SY; Shakhnazarova AA
Vestn Oftalmol; 2019; 135(6):91-99. PubMed ID: 32015313
[TBL] [Abstract][Full Text] [Related]
25. A novel mutation in the PAX3 gene causes Waardenburg syndrome type I in an Iranian family.
Jalilian N; Tabatabaiefar MA; Farhadi M; Bahrami T; Noori-Daloii MR
Int J Pediatr Otorhinolaryngol; 2015 Oct; 79(10):1736-40. PubMed ID: 26279250
[TBL] [Abstract][Full Text] [Related]
26. A rare case of seven siblings with Waardenburg syndrome: a case report.
Haj Kassem L; Ahmado MF; Sheikh Alganameh M
J Med Case Rep; 2018 Jul; 12(1):192. PubMed ID: 29973257
[TBL] [Abstract][Full Text] [Related]
27. Identification of a Novel De Novo Variant in the PAX3 Gene in Waardenburg Syndrome by Diagnostic Exome Sequencing: The First Molecular Diagnosis in Korea.
Jang MA; Lee T; Lee J; Cho EH; Ki CS
Ann Lab Med; 2015 May; 35(3):362-5. PubMed ID: 25932447
[TBL] [Abstract][Full Text] [Related]
28. Waardenburg syndrome type 3 (Klein-Waardenburg syndrome) segregating with a heterozygous deletion in the paired box domain of PAX3: a simple variant or a true syndrome?
Tekin M; Bodurtha JN; Nance WE; Pandya A
Clin Genet; 2001 Oct; 60(4):301-4. PubMed ID: 11683776
[TBL] [Abstract][Full Text] [Related]
29. A Novel
Li S; Guo M; Ruan B; Liu Y; Cui X; Han W; Li R
Genet Test Mol Biomarkers; 2020 May; 24(5):249-255. PubMed ID: 32250160
[No Abstract] [Full Text] [Related]
30. Waardenburg syndrome.
Bist J; Adhikari P; Sharma AK
Clin Exp Optom; 2011 Mar; 94(2):240-2. PubMed ID: 21352370
[No Abstract] [Full Text] [Related]
31. Pigmentary anomalies and hearing loss.
Toriello HV
Adv Otorhinolaryngol; 2011; 70():50-55. PubMed ID: 21358185
[TBL] [Abstract][Full Text] [Related]
32. Molecular and clinical characterization of Waardenburg syndrome type I in an Iranian cohort with two novel PAX3 mutations.
Jalilian N; Tabatabaiefar MA; Farhadi M; Bahrami T; Emamdjomeh H; Noori-Daloii MR
Gene; 2015 Dec; 574(2):302-7. PubMed ID: 26275939
[TBL] [Abstract][Full Text] [Related]
33. Waardenburg syndrome: iris and choroidal hypopigmentation: findings on anterior and posterior segment imaging.
Shields CL; Nickerson SJ; Al-Dahmash S; Shields JA
JAMA Ophthalmol; 2013 Sep; 131(9):1167-73. PubMed ID: 23868078
[TBL] [Abstract][Full Text] [Related]
34. Multimodal Ultrawide-Field Imaging Features in Waardenburg Syndrome.
Choudhry N; Rao RC
Ophthalmic Surg Lasers Imaging Retina; 2015 Jun; 46(6):670-3. PubMed ID: 26114849
[TBL] [Abstract][Full Text] [Related]
35. Effects of Pax3 modifier genes on craniofacial morphology, pigmentation, and viability: a murine model of Waardenburg syndrome variation.
Asher JH; Harrison RW; Morell R; Carey ML; Friedman TB
Genomics; 1996 Jun; 34(3):285-98. PubMed ID: 8786127
[TBL] [Abstract][Full Text] [Related]
36. Novel PAX3 mutations causing Waardenburg syndrome type 1 in Tunisian patients.
Trabelsi M; Nouira M; Maazoul F; Kraoua L; Meddeb R; Ouertani I; Chelly I; Benoit V; Besbes G; Mrad R
Int J Pediatr Otorhinolaryngol; 2017 Dec; 103():14-19. PubMed ID: 29224756
[TBL] [Abstract][Full Text] [Related]
37. A del(13)(q21.32q31.2)dn refined to 21.9 Mb in a female toddler with irides heterochromia and hypopigmentation: appraisal of interstitial mid-13q deletions.
Córdova-Fletes C; Rivera H; Garza-Villarreal EA; Vázquéz-Cárdenas NA; Martínez-Jacobo LA; Moreno-Andrade T
Clin Dysmorphol; 2017 Jan; 26(1):33-37. PubMed ID: 27750267
[No Abstract] [Full Text] [Related]
38. Congenital deafness with pigmentary disturbance of the irides.
Ghoshal L; Barua JK; Biswas A
J Paediatr Child Health; 2014 Aug; 50(8):655. PubMed ID: 25080984
[No Abstract] [Full Text] [Related]
39. Case report: waardenburg syndrome.
Dumayas GL; Capó-Aponte JE
Mil Med; 2015 Mar; 180(3):e381-7. PubMed ID: 25735036
[TBL] [Abstract][Full Text] [Related]
40. Asymmetric choroidal hypopigmentation in a Son and mother with Waardenburg syndrome type I.
Grewal PS; Knight H; Michaelides M
Ophthalmic Genet; 2020 Jun; 41(3):284-287. PubMed ID: 32281454
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
